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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620930Generated: November 3, 2026

Acetic Anhydride → HCID 57446943, compound

https://huagongshe.com/reaction/1620930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
Reactant5,5,5-trifluoroleucine HCl saltHCID 71359846—
SolventWaterHCID 962—
ProductHCID 57446943HCID 57446943—

Reaction Steps

To a cold (0° C.) solution of the 5,5,5-trifluoroleucine HCl salt (from Step 1 above) in H2O (30 mL) was added 1M aqueous NaOH (60 mL, 60 mmol) followed by acetic anhydride (3.5 mL, 36.7 mmol). The mixture was stirred at room temperature for 30 min to 1 h. After acidification with 6M aqueous HCl (6 mL), the mixture was extracted with EtOAc (6×). The combined EtOAc extracts were washed with brine, dried (MgSO4) and concentrated. The residue was swished with hexanes:Et2O (1:1) to afford N-acetyl-5,5,5-trifluoroleucine as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772336B2
Source datasetuspto-grants-2014_07
ORD IDord-1097263f507643e28a936edefcb5f73f
Source noteuspto-grants-2014_07